Why Should I Register and Submit Results? EXPEDIUM OffSET SURGICAL TECHNIQUE pEdIcLE HooKS The hook driver can be used in conjunction with the open hook holder to position the pedicle hook. The rate of Adverse Events must be no worse than in the control group as well. Miami Children’s Hospital Miami, Florida Building upon decades of cumulative design history, sound surgical philosophy, clinical experience and biomechanical performance of the MOSS ®, MOSS MIAMI and MOSS MIAMI ® remove the reduction Tube and Clip-On Device. Phase 3. Information provided by (Responsible Party): The purpose of this study is to determine the clinical success of DePuy Spine Titanium Surgical Mesh with MOSS Miami Spinal Fixation System Pedicle Screws in the treatment of one or two levels of degenerative disc disease of the lumbar spine. Adjustable nose beam and procedure ear loops, Developed for hospitals, laboratories, food industry, nursing and doctor's offices. U.S. Department of Health and Human Services, The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Our experts in materials, technology and technique are now manufacturing personal protective equipment to help solve personal health needs. For general information, Learn About Clinical Studies. Developed to meet ASTM F2100 standard, Bacterial Filtration Efficiency (BFE) > 98%, Free from natural rubber latex and fiberglass, Securely welded procedural ear loops and adjustable nose beam, Downloads: Datasheet, Spec sheet, Why this Surgical Mask, Comfortable foam at brows allows space for mask and glasses, Adjustable 1” Velcro strap allows for a secure fit and a universal size, Adjustable nose beam and elastic ear loops. Operating on three continents, we have unsurpassed experience, capacity, and reach in delivering solutions for any venue at any size, anywhere. Moss provides reliability and sustainability through ever-advancing process and solution innovations. Surgical Titanium Mesh™ with MOSS-Miami™ Pedicle Screws, Device: Lumbar I/F with cage and pedicle screws. 10501 Seymour Ave. Franklin Park, IL 60131(800) 341-1557. Freedom from Secondary Surgical Intervention. Daily Herald - Moss to Triple Surgical Mask Production, WGN Radio - Interview of Moss CEO Dan Patterson on Procedure Face Mask Initiative, WBBM Newsradio - Interviews Moss CEO Dan Patterson on Procedure Face Mask PivotEXHIBITOR - Moss Producing Personal Protective Equipment, VMSD - COVID19: Moss Pivots to Produce PPE, AUTOMATED PRODUCTION LINES IN THE U.S.A. AND GERMANY. CBS Chicago - What Makes American Made Masks More Trustworthy Than Others? The rod is captured into the pedicle hook by inserting the set screws. Blending materials, technology and technique, Moss is a limitless one-stop shop for turning visionary design into amazing reality. Moss partners with brands around the world to tell their story through compelling experiences. Developed for hospitals, laboratories, food industry, nursing and doctor's offices. Made in the U.S.A. with Imported Materials, EXHIBITOR - Moss Producing Personal Protective Equipment, By subscribing, you are signing up to receive email updates and special offers from Moss, The information you've provided will be used in accordance with the terms of our, WBBM Newsradio - Interviews Moss CEO Dan Patterson on Procedure Face Mask Pivot.
Capture the rod by threading the Single Innie into the implant head until tight. Surgical Technique Guide IntroductIon Behrooz A. Akbarnia, MD San Diego Center for Spinal Disorders La Jolla, California Oheneba Boachie-Adjei, MD Hospital for … Final tightening is performed, utilizing the open hook stabilizer, and tightening the set screw to 80 inch pounds. Moss is scaling capacity in Europe and North America to produce a global output of 6 million masks per week.
Surgical Technique ACTIS Total Hip System DePuy Synthes 9 It is always recommended that you introduce the femoral stem as far as possible by hand before using a stem inserter.
The observed success rate at 24 months will be compared to an historical control group treated with the Lumbar I/F Cage with VSP System. Across three continents, Moss partners with brands around the world to tell their stories through compelling experiences.
COVID-19 is an emerging, rapidly evolving situation. SUrGICaL TECHNIUE GUIDE Thread the reduction Tube into the Clip-On Device to fully seat the rod. Read our, ClinicalTrials.gov Identifier: NCT00215319, Interventional Infection in the disc or spine, past or present. Please remove one or more studies before adding more. Blending materials, technology and technique, Moss is a limitless one-stop shop for turning visionary design into amazing reality. Across three continents, Moss partners with brands around the world to tell their stories through compelling experiences. Choosing to participate in a study is an important personal decision.
This is a single arm multi-center study to determine the clinical success of the DePuy Spine Titanium Surgical Mesh with MOSS Miami Spinal Fixation System Pedicle Screws in the treatment of one or two adjacent levels of degenerative disc disease of the lumbar spine (L2 - S1). Listing a study does not mean it has been evaluated by the U.S. Federal Government. About Moss partners with brands around the world to tell their story through compelling experiences. Study Success is as a compound endpoint requiring: Results will be compared to an historical control group treated with the Lumbar I/F Cage with VSP System. Prior fusion surgery of the lumbar spine; prior discectomies or IDET allowed. We are a proven partner for every brand presentation possibility. To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. Significant osteoporosis or metabolic bone disease. Radiographic evidence of significant disc degeneration at one or two of the adjacent lumbar levels L2-S1. Detailed Description: This is a single arm multi-center study to determine the clinical success of the DePuy Spine Titanium Surgical Mesh with MOSS Miami Spinal Fixation System Pedicle Screws in the treatment of one or two adjacent levels of … The health and personal safety of medical service providers, first responders and many others is our global community's number one priority. Get the latest research information from NIH: You have reached the maximum number of saved studies (100). Greater than Grade I spondylolisthesis or significant bony defect in the lumbar spine. Moss has invested in high speed manufacturing systems for 3-ply face masks. Persistent back and/or leg pain refractory to 6 months of non-surgical therapy. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00215319. Talk with your doctor and family members or friends about deciding to join a study. Study record managers: refer to the Data Element Definitions if submitting registration or results information.
Pregnant or lactating, or wishes to become pregnant within duration of study. (Clinical Trial), A Multi-center Study to Evaluate the Safety and Efficacy of DePuy AcroMed Titanium Surgical Mesh and MOSS-Miami Spinal Fixation System Pedicle Screws for Intradiscal Fusion in the Lumbar Spine, 18 Years to 79 Years (Adult, Older Adult), Fort Wayne, Indiana, United States, 46825, Degenerative disc disease at up to 2 levels (L2-S1), Maintenance/Improvement in Neurologic Status, and. Through global sourcing, fabrication, printing and technical design, Moss creates elevated brand environments that emotionally and powerfully connect with a brand’s community. Our experts in materials, technology and technique are now manufacturing personal protective equipment to solve public health needs.
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